WO2001081647A2 - Poudre a pulveriser amelioree resistant a la chaleur - Google Patents

Poudre a pulveriser amelioree resistant a la chaleur Download PDF

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Publication number
WO2001081647A2
WO2001081647A2 PCT/US2001/012676 US0112676W WO0181647A2 WO 2001081647 A2 WO2001081647 A2 WO 2001081647A2 US 0112676 W US0112676 W US 0112676W WO 0181647 A2 WO0181647 A2 WO 0181647A2
Authority
WO
WIPO (PCT)
Prior art keywords
microns
chromium oxide
particles
powder
process according
Prior art date
Application number
PCT/US2001/012676
Other languages
English (en)
Other versions
WO2001081647A3 (fr
Inventor
Howard Wallar
Robert F. Quinlivan
Sung H. Yu
Original Assignee
Saint-Gobain Ceramics & Plastics, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=24220854&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2001081647(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Saint-Gobain Ceramics & Plastics, Inc. filed Critical Saint-Gobain Ceramics & Plastics, Inc.
Priority to EP09153604.5A priority Critical patent/EP2062993B1/fr
Priority to BRPI0110217-6A priority patent/BR0110217B1/pt
Priority to DE60139120T priority patent/DE60139120D1/de
Priority to MXPA02010467A priority patent/MXPA02010467A/es
Priority to JP2001578714A priority patent/JP3917425B2/ja
Priority to CA002403653A priority patent/CA2403653C/fr
Priority to EP01928636A priority patent/EP1276916B1/fr
Priority to AT01928636T priority patent/ATE435313T1/de
Publication of WO2001081647A2 publication Critical patent/WO2001081647A2/fr
Publication of WO2001081647A3 publication Critical patent/WO2001081647A3/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/12—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on chromium oxide
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/10—Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
    • C23C4/11—Oxides
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G37/00—Compounds of chromium
    • C01G37/02—Oxides or hydrates thereof
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/01—Particle morphology depicted by an image
    • C01P2004/03—Particle morphology depicted by an image obtained by SEM
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/51—Particles with a specific particle size distribution
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/60—Particles characterised by their size
    • C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer

Definitions

  • the present invention relates to thermal spray po ders and specifically to chromium oxide thermal spray powders. It is known in the art that it is highly advantageous to apply a fine coating of a ceramic metal oxide to substrates that are, in use, subjected to high temperatures or to highly abrasive or corrosive environments so as to protect the surface of the metal from wear damage or physical deterioration.
  • These coatings can be applied in a variety of ways but among the more frequently used are oxygen fuel guns such as the detonation gun, (the "D-Gun”), manufactured and sold by Praxair; and high-velocity oxygen fuel (“HVOF”) guns such as those manufactured and sold by Sulzer-Metco, Praxair, TAFA and plasma guns manufactured by SNMI, Sulzer-Metco, Praxair, TAFA and others.
  • oxygen fuel guns such as the detonation gun, (the "D-Gun"), manufactured and sold by Praxair; and high-velocity oxygen fuel (“HVOF”) guns such as those manufactured and sold by Sulzer-Metco, Praxair, TAFA and plasma guns manufactured by SNMI, Sulzer-Metco, Praxair, TAFA and others.
  • HVOF high-velocity oxygen fuel
  • the size parameter is particularly important since a uniform coating is required and because the systems often have trouble handling widely different particle sizes in the same feed.
  • thermal spray powders have particle sizes from 5 to 125 microns but any particular powder used will have a rather narrow particle size variation within this broad range.
  • graded sizes such as 5-25, 10-30, 10-38, 15-45, 22-45, 10-63, 45-75, 45- 125 and so on. In such graded sizes fines are avoided as far as possible with a fines tolerance usually being specified at no more than 2 to 5% below the bottom limit. Wherever possible particle sizes below 5 microns are removed to increase productivity.
  • This narrow size distribution is important to optimize melting and delivery of material to the gun at a uniform rate. Fine particles tend to hamper flow and/or cause nozzle build-up during application. They also tend to cause irregular flow and to stick to the surface of larger particles. All this results in uneven coating and build-up rate and when this is detected the process must be shut down and corrective measures taken. If it is not detected a defect, such as the deposition of agglomerates of fine particles, can result in pinholes, large pores or defects which in turn can lead to coating failure or, if detected, require re-working. Thus a narrow particle size range with a minimum of associated fines is critical in providing a high quality thermal spray powder.
  • thermal spray powders are also important in their effective and economic use. Rounded shapes are best with blocky shapes also being quite acceptable. However shapes that are weak, that is having a distinct aspect ratio, (the ratio of the longest particle dimension to the next longest dimension perpendicular to the longest), of about 2 or more, can cause severe flow problems and therefore irregular coatings.
  • the ideal powder for thermal spray applications is round and falls within a narrow size range and has a minimum of fines outside that range.
  • the chemical nature of the powder is determined by the application for which it is intended. Where such application is intended to impart wear resistance, strength, corrosion resistance and suitability for laser engraving for example, the powder of choice is chromium oxide. Such powders have their own specific problem in such applications since they are often contaminated by chromium metal which must be reduced to a minimum, usually below 0.1% by weight, before they can be used.
  • Chromium oxide is typically produced in a fusion process in an electric arc furnace using a feed of fine pigment-grade chromium oxide with a particle size of about 3 microns.
  • the fusion process causes the particles to melt and fuse into an ingot that is then crushed to the appropriate particle sizes.
  • the arc furnace which uses carbon electrodes, operates under somewhat reducing conditions leaving a significant amount of chromium metal as an impurity. This can be reduced to acceptable levels by subsequent calcination under oxidizing conditions.
  • the ingot of fused chromium oxide is milled to produce a fine powder which is then size-classified and the desired particle size range is heated in a furnace at temperatures above about 1100°C in a flow of air. Any resulting agglomeration can readily be broken down to the ultimate particles again by a light milling.
  • the fusion process is somewhat expensive and results in the loss of the considerable amount of fines, material that is typically removed prior to calcination. These fines are often recycled through the fusion process or otherwise disposed of.
  • a process for making an improved chromium oxide thermal spray powder has now been devised that is more economical, results in particles with a better shape and involves less unusable by-product.
  • the process has an added degree of flexibility in making surface chemistry adjustments in the particles and therefore the coating applied.
  • the present invention provides a process for the production of a chromium oxide thermal spray powder which comprises calcining chromium oxide powder with particle size range of 0.1 to 125 microns and comprising at least 5% by volume of chromium oxide particles smaller than 10 microns for a time sufficient to reduce the volume of particles with sizes less than 10 microns to below 5%, and preferably below 2%, of the total weight of chromium oxide.
  • chromium oxide particles are usually made by fusing pure chromium oxide in an electric arc furnace. This is because the fine particles, which are too fine to use directly in thermal spray applications, do not readily sinter together. Rather the surface material tends to volatilize and then - condense. This explains the previous commercial practice of fusing, crushing and fines segregation as discussed above..
  • a preferred process therefore comprises: a) feeding chromium oxide particles with sizes of from 0.1 to 125 microns into a furnace along with from 0 to 100% based on the weight of the comminuted product, of chromium oxide powder with a particle size less than 10 microns to produce a mixture of particles in which at least 5% by volume of the particles are smaller than 10 microns; b) calcining the mixture at a temperature above 1000°C for a time sufficient to cause reduction of the content of chromium oxide particles smaller than 10 microns to below 5% ; and c) cooling and classifying the resultant product.
  • the mixture comprises chromium metal
  • the calcining operation be carried out in an air flow to cause oxidation of the metal to the oxide.
  • the initial charge of chromium oxide is obtained by a fusion process producing a block of chromium oxide followed by a comminution of the block until the particle size is below 125 microns.
  • This process has the advantage that the powder obtained by crashing the fused chromium oxide does not need to be classified to remove fines before calcination and, by using the fine powder feedstock used to make the fused chromium oxide powder, the process throughput in greatly increased.
  • the fines produced by the comminution and the new fine powder added are used to improve the shape of the chromium oxide particles and render them closer to the spherical.
  • fused particles as sites allows the reaction with fine particles to take place at relatively low temperatures above 1100°C and preferred at 1350°C.
  • the reaction will also take place when using 100% of particles less than 10 microns providing a protracted time at low temperatures or increased temperature is used.
  • increased temperature in the range of 1600C, product of 5 to 125 microns from feeds ⁇ 10 microns can be made in reasonable times without the need for larger fused particles as sites for growth.
  • Drawings Figure 1 is an SEM photomicrograph of chromium oxide particles after comminution but before calcination.
  • Figure 2 is an SEM photomicrograph of chromium oxide particles as shown in
  • Figure 3 is a graph showing Microtrac particle sizes before and after calcination as described in Example 1, Table 1, "Milled Feed Alone"
  • Figures 4 and 5 are, respectively, pre- and post-calcination SEM photomicrographs of the products made according to Example 6.
  • Figures 6 and 7 are, respectively, pre- and post-calcination SEM photomicrographs of the products made according to Example 7.
  • Figures 8 and 9 are, respectively, pre- and post-calcination SEM photomicrographs of the products made according to Example 8.
  • the comminuted chromium oxide was obtained by fusing chromium oxide powders with particle sizes primarily below 10 microns in an electric arc furnace with carbon electrodes to form an ingot of chromium oxide which was then comminuted using a rolls crusher.
  • Fusion of fine chromium oxide particles was carried out in a conventional carbon arc fusion furnace operated at a temperature of 2800°C.
  • This Table sets out the results of calcining a feed obtained directly from a roller mill crusher without the customary separation of fines.
  • the second evaluation was performed on a separated fines fraction from a roller mill crasher having a D 50 of about 3 to 5 microns, ("milled fines") with the addition of 10% of pigment grade chromium oxide which also had a D 50 of about 3 microns, (“fines").
  • This added material is the same chromium oxide used as the feedstock for the fusion process by which the chromium oxide fed to the roll crusher was made. For each, the initial, or "green”, particle size distribution and the "fired” particle size distribution are given.
  • the upper portion of the Table gives the D ⁇ 0 , D 50 and D 90 values and the values given in the lower part of the Table indicate the percentage of particles with sizes smaller than the indicated value in the lower part of the left hand column. It will be readily apparent that the particle size distribution has shifted markedly towards the larger particle sizes and the particles below about 5 microns have been virtually eliminated.
  • Example 2 The following Example is similar to that set forth in Example 1 with the difference that the two feeds evaluated were based on a classified roller mill product wherein all particles had a particle size less than 50 microns and to which an amount of the same pigment grade chromium oxide as used in Example 1 had been added. The amount added was either 10% or 25% by weight of the milled feed. The results obtained are shown in Table 2.
  • Examples 5-7 illustrate variations in the site materials. Adding pigment grade chromium oxide to alumina, zirconia, spinel, chromium oxide and many other site particles can make a layered chemistry particle where the core is the site particle and chromium oxide is the outer layer. Other chemistries like alumina or spinel or zirconia or iron oxide can be added to the fine chromium oxide for an infinitely variable surface chemistry product. In addition the core particle can be changed for more variation in chemistry.
  • FIG. 4 shows the use of a spinel particle as the core or site material representing 50 % of the mix with 50% chromium oxide fines added.
  • Figures 4 and 5 are photomicrographs of the pre- and post-calcination products. The particles size distributions are shown in the following Table.
  • Example core particles comprising 6%Yttria- ⁇ 9%zircoma-25%alumina are treated to give a coating of chromia.
  • the particle size distribution before and after calcination is given in the following Table. ' The core particles represented
  • chromium oxide pigment 50% by weight and chromium oxide pigment provided the balance of the weight.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Physics & Mathematics (AREA)
  • Plasma & Fusion (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Structural Engineering (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Coating By Spraying Or Casting (AREA)
  • Manufacturing Of Micro-Capsules (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

On a remarqué que le fait de calciner des poudres d'oxyde de chrome formées d'un constituant ayant une grosseur particulaire inférieure à 10 microns a pour effet de réduire la proportion en volume des particules plus petites et d'accroître l'uniformité globale des grosseurs particulaires au niveau de la distribution et de la rondeur des particules.
PCT/US2001/012676 2000-04-24 2001-04-19 Poudre a pulveriser amelioree resistant a la chaleur WO2001081647A2 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
EP09153604.5A EP2062993B1 (fr) 2000-04-24 2001-04-19 Procédé de fabrication de poudre à pulvériser
BRPI0110217-6A BR0110217B1 (pt) 2000-04-24 2001-04-19 processo para a produção de um pó de óxido de cromo.
DE60139120T DE60139120D1 (de) 2000-04-24 2001-04-19 Sprühpulver
MXPA02010467A MXPA02010467A (es) 2000-04-24 2001-04-19 Polvo de aspersion termica mejorado.
JP2001578714A JP3917425B2 (ja) 2000-04-24 2001-04-19 改良された溶射粉末の製造方法
CA002403653A CA2403653C (fr) 2000-04-24 2001-04-19 Poudre a pulveriser amelioree resistant a la chaleur
EP01928636A EP1276916B1 (fr) 2000-04-24 2001-04-19 Poudre a pulveriser
AT01928636T ATE435313T1 (de) 2000-04-24 2001-04-19 Sprühpulver

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/556,324 2000-04-24
US09/556,324 US6410470B1 (en) 2000-04-24 2000-04-24 Thermal spray powder process

Publications (2)

Publication Number Publication Date
WO2001081647A2 true WO2001081647A2 (fr) 2001-11-01
WO2001081647A3 WO2001081647A3 (fr) 2002-02-21

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ID=24220854

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PCT/US2001/012676 WO2001081647A2 (fr) 2000-04-24 2001-04-19 Poudre a pulveriser amelioree resistant a la chaleur

Country Status (11)

Country Link
US (1) US6410470B1 (fr)
EP (2) EP2062993B1 (fr)
JP (1) JP3917425B2 (fr)
KR (1) KR100499743B1 (fr)
AT (1) ATE435313T1 (fr)
BR (1) BR0110217B1 (fr)
CA (1) CA2403653C (fr)
DE (1) DE60139120D1 (fr)
ES (1) ES2329441T3 (fr)
MX (1) MXPA02010467A (fr)
WO (1) WO2001081647A2 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7012037B2 (en) 2002-04-08 2006-03-14 Saint-Gobain Ceramics And Plastics, Inc. Chromia spray powders
EP2062993A1 (fr) 2000-04-24 2009-05-27 Saint-Gobain Ceramics and Plastics, Inc. Poudre à pulvériser

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US6774076B2 (en) * 2002-04-08 2004-08-10 Saint-Gobain Ceramics & Plastics, Inc. Chromia spray powders and a process for making the same
FR2844448B1 (fr) 2002-09-17 2006-06-23 Lcw Les Colorants Wackherr Methode de preparation extemporanee de compositions cosmetiques ayant la texture d'une creme, et compositions pour la mise en oeuvre de cette methode
FR2844800B1 (fr) * 2002-09-19 2006-07-21 Pigments d'oxyde de chrome a teneur reduite en chrome(vi)
EP1510593A1 (fr) * 2003-08-28 2005-03-02 Siemens Aktiengesellschaft Procédé pour revêtir un objet, objet et poudre
JP4885445B2 (ja) * 2004-12-21 2012-02-29 株式会社フジミインコーポレーテッド 溶射用粉末
CA2619331A1 (fr) * 2007-01-31 2008-07-31 Scientific Valve And Seal, Lp Revetements, leur fabrication et utilisation
US20090162273A1 (en) * 2007-12-21 2009-06-25 Howmedica Osteonics Corp. Chromium oxide powder having a reduced level of hexavalent chromium and a method of making the powder
JP5889564B2 (ja) * 2011-07-26 2016-03-22 オーエスジー株式会社 工具の表面改質方法
DE102017218580A1 (de) * 2017-10-18 2019-04-18 Christian Maier GmbH & Co. KG Verfahren zum Aufbringen einer Schicht auf ein Bauteil und Bauteil hergestellt nach dem Verfahren

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2062993A1 (fr) 2000-04-24 2009-05-27 Saint-Gobain Ceramics and Plastics, Inc. Poudre à pulvériser
US7012037B2 (en) 2002-04-08 2006-03-14 Saint-Gobain Ceramics And Plastics, Inc. Chromia spray powders

Also Published As

Publication number Publication date
JP3917425B2 (ja) 2007-05-23
MXPA02010467A (es) 2003-04-25
EP1276916A2 (fr) 2003-01-22
KR100499743B1 (ko) 2005-07-07
CA2403653A1 (fr) 2001-11-01
EP2062993B1 (fr) 2019-06-26
EP1276916B1 (fr) 2009-07-01
US6410470B1 (en) 2002-06-25
BR0110217A (pt) 2003-01-21
ES2329441T3 (es) 2009-11-26
BR0110217B1 (pt) 2011-04-05
EP2062993A1 (fr) 2009-05-27
WO2001081647A3 (fr) 2002-02-21
ATE435313T1 (de) 2009-07-15
CA2403653C (fr) 2006-06-20
KR20020093060A (ko) 2002-12-12
DE60139120D1 (de) 2009-08-13
JP2003531298A (ja) 2003-10-21

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